Our mission is to become a worldwide reference for education in the field for all professionals involved in the process to dissemintate knowledge & skills of Acute Cardiovascular Care
Our mission is to promote excellence in clinical diagnosis, research, technical development, and education in cardiovascular imaging in Europe.
Our mission: To promote excellence in research, practice, education and policy in cardiovascular health, primary and secondary prevention.
Our goal is to reduce the burden in cardiovascular disease in Europe through percutaneous cardiovascular interventions.
Our Mission is "to improve the quality of life of the population by reducing the impact of cardiac rhythm disturbances and reduce sudden cardiac death"
To improve quality of life and logevity, through better prevention, diagnosis and treatment of heart failure, including the establishment of networks for its management, education and research.
Working Groups goals is to stimulate and disseminate scientific knowledge in different fields of cardiology.
ESC Councils goal is to share knowledge among medical professionals practising in specific cardiology domains.
OUR MISSION: TO REDUCE THE BURDEN OF CARDIOVASCULAR DISEASE
The primary objective of the Heart Failure Registry is to describe the clinical epidemiology of outpatients and inpatients with Heart Failure and the diagnostic/therapeutic processes (including the organization of Heart Failure management programmes) applied to these patients across Europe and Mediterranean countries.
To describe the demographic, clinical, and biological characteristics of outpatients and inpatients with Heart Failure (HF) followed by a representative setting of cardiology centres.
Specific attention will be focused on:
More than 30 countries are taking part in this registry, which was launched in May 2011.
The aim of enrolling approximately 10,000 patients during the first year has been achieved.
Prior to the deployment of the long-term registry a pilot registry was conducted, between October 2009 and May 2010, with a one-year follow-up. This pilot study was specifically aimed at validating the structure, performance, and quality of the data set, for continuing the survey into a permanent registry.12 countries enrolled 5118 patients in this pilot, of which the first results were presented at the ESC Congress 2010.
If you are already registered as a participant in the EORP programme, you may connect to our secure website: http://www.eorp.org
Marisa Crespo Leiro (Chair)Alexandre MebazaaMassimo PiepoliAndrew CoatsStefan AnkerGerasimos FilippatosAldo Maggioni
Aldo Maggioni (Chairman)Stefan AnkerUlf DahlströmGerasimos FilippatosLuigi TavazziPiotr PonikowzkiFaiez Zannad
The Steering Committee is composed of one National Coordinator per participating country. The National Societies are responsible for the selection of the national coordinators and participating centres.Steering Committee members
Friedrich Fruhwald (AT)Emir Fazlibegovic (BA)Plamen Gatzov (BG)Davor Milicic (HR)Theodoros Christodoulides (CY)Jaromir Hradec (CZ)Tiina Uuetoa (EE)Mahmoud Hassanein (EG)Damien Logeart, Richard Isnard (FR)Vakhtang Chumburidze (GE)Dimitris Tousoulis (GR)Béla Merkely (HU)Offer Amir (IL)Marco Metra (IT)Andrejs Erglis (LV)Ausra Kavoliuniene (LT)Elizabeta Srbinovska, Magdalena Otljanska (MK)Eleonora Vataman (MD)Jaroslaw Drozdz (PL)Candida Fonseca (PT)Ovidiu Chioncel (RO)Evgeny Shkolnik (RU)Milica Dekleva (RS)Eva Goncalvesova (SK)Mitja Lainscak (SI)Juan Delgado Jimenez (SP)Ulf Dahlström (SE)Ahmet Temizhan (TR)
Aldo Maggioni (Chairman) Ulf DahlströmGerasimos FilippatosLuigi TavazziFaiez Zannad
Friedrich Fruhwald (AT)Mathias Rauchhaus (DE)Olav Wendelboe Nielsen (DK)Marisa Crespo-Leiro (ES)Damien Logeart (FR)John T. Parissis (GR)Marco Metra (IT)Adrian A. Voors (NL)Lars Gullestad (NO)Jaroslaw Drozdz (PL)Ovidiu Chioncel (RO)Hans Persson (SE)